Canonical Allele Identifier: CA1441591529
Gene: QDPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17504410T= , CM000666.2:g.17504410T= GRCh38
NC_000004.11:g.17506033T= , CM000666.1:g.17506033T= GRCh37
NC_000004.10:g.17115131T= NCBI36
NG_008763.1:g.12825A=

Transcript Alleles

HGVS Amino-acid change
ENST00000706645.1:n.1311A=
ENST00000281243.10:c.264A= MANE Select ENSP00000281243.5:p.Gly88=
ENST00000281243.9:c.264A= ENSP00000281243.5:p.Gly88=
ENST00000428702.6:c.171A= ENSP00000390944.2:p.Gly57=
ENST00000505710.1:c.191A=
ENST00000507439.5:c.264A= ENSP00000423227.1:p.Gly88=
ENST00000508623.5:c.264A= ENSP00000426377.1:p.Gly88=
ENST00000513615.5:c.264A= ENSP00000422759.1:p.Gly88=
ENST00000514300.1:c.*195A= ENSP00000426039.1:n.*195A=
NM_000320.2:c.264A= NP_000311.2:p.Gly88=
NM_001306140.1:c.171A= NP_001293069.1:p.Gly57=
XR_241677.1:n.427A=
NR_156494.1:n.444A=
NM_000320.3:c.264A= MANE Select NP_000311.2:p.Gly88=
NM_001306140.2:c.171A= NP_001293069.1:p.Gly57=
NR_156494.2:n.300A=